Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1020581000172119 | maladie de Charcot-Marie-Tooth type 2H | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3321619016 | Charcot-Marie-Tooth disease type 2H (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3321620010 | Charcot-Marie-Tooth disease type 2H | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3321621014 | Axonal Charcot-Marie-Tooth disease with pyramidal involvement | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 755811000241113 | maladie de Charcot-Marie-Tooth type 2H (trouble) | fr | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 885451000172111 | AR-CMT2C - autosomal recessive Charcot-Marie-Tooth disease type 2C | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3321622019 | An axonal peripheral sensorimotor polyneuropathy associated with pyramidal involvement. So far, it has been described in 13 members of a large Tunisian family. Onset occurred during the first decade of life with progressive distal atrophy involving both the upper and lower limbs, associated with a mild pyramidal syndrome (brisk patellar and upper limb reflexes, absent ankle reflexes and unattainable plantar reflexes). Transmitted in an autosomal recessive manner and the disease-causing locus has been mapped to 8q13-21.1. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| maladie de Charcot-Marie-Tooth type 2H | est un(e) (attribut) | Autosomal recessive Charcot-Marie-Tooth disease type 2 | true | Inferred relationship | Some | ||
| maladie de Charcot-Marie-Tooth type 2H | est un(e) (attribut) | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
| maladie de Charcot-Marie-Tooth type 2H | est un(e) (attribut) | Charcot-Marie-Tooth disease, type II (disorder) | false | Inferred relationship | Some | ||
| maladie de Charcot-Marie-Tooth type 2H | localisation d'une constatation (attribut) | structure du système nerveux périphérique | true | Inferred relationship | Some | 1 | |
| maladie de Charcot-Marie-Tooth type 2H | morphologie associée (attribut) | atrophie (anomalie morphologique) | true | Inferred relationship | Some | 2 | |
| maladie de Charcot-Marie-Tooth type 2H | localisation d'une constatation (attribut) | structure d'un nerf | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR